General Information of This Metabolic Reaction (MR) (ID: MR012915)
Formula
SVG example
Reactant NSC-63853 Product Androsterone
Reactant Info Product Info
Other MR(s) Related to The Reactant of This MR
Other MR(s) That Metabolize The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR012911 NSC-63853 17-alpha-hydroxyprogesterone Unclear NSC-63853 [1]
MR012916 NSC-63853 Cortisol Unclear NSC-63853 [2]
MR012912 NSC-63853 Dehydroepiandrosterone Unclear NSC-63853 [3]
MR012914 NSC-63853 Etiocholanolone Unclear NSC-63853 [4]
MR012913 NSC-63853 Isoandrosteron Unclear NSC-63853 [4]
Other MR(s) Related to The Product of This MR
Other MR(s) That Produce The Product of This MR
MR ID Reactant Product MR Type Related Drug REF
MR007036 Hombreol Androsterone Oxidation - Oxidationn Hombreol [5]
References
1 CONVERSION OF 17-ALPHA-HYDROXYPREGNENOLONE TO 17-ALPHA-HYDROXYPROGESTERONE BY THE CANINE TESTIS IN VIVO
2 The conversion in vitro of 17-hydroxypregnenolone to cortisol by a human adrenal tumor
3 The role of cytochrome b5 in the biosynthesis of androgens by human P450c17
4 The conversion in vivo of 17-alpha-hydroxypregnenolone to dehydroisoandrosterone and other 17-ketosteroids
5 Transcriptional regulation of type 11 17beta-hydroxysteroid dehydrogenase expression in prostate cancer cells. Mol Cell Endocrinol. 2011 Jun 6;339(1-2):45-53.

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